二元结果效果测度的选择:引入反事实结果状态转换参数。

Q3 Mathematics
Epidemiologic Methods Pub Date : 2018-12-01 Epub Date: 2018-07-27 DOI:10.1515/em-2016-0014
Anders Huitfeldt, Andrew Goldstein, Sonja A Swanson
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引用次数: 14

摘要

标准的效果衡量标准,包括风险比、比值比和风险差,与许多被充分描述的缺点有关,对于研究人员应该选择一种效果衡量标准而不是另一种效果测量标准的条件,没有达成共识。在本文中,我们引入了一个新的框架,通过将风险比的两个不同版本与反事实因果模型联系起来,来推理效果度量的选择。在我们的方法中,效应是根据“反事实结果-状态转换参数”来定义的,即如果不治疗,在随访结束时不会成为病例的个体的比例,他们会通过成为病例来对治疗做出反应;以及如果不治疗,在随访结束时会成为病例的人中,对治疗有反应的人不会成为病例的比例。尽管在没有强单调性假设的情况下,通常不会从数据中识别出反事实的结果-状态转换参数,但我们表明,当它们在人群之间保持不变时,对模型规范、荟萃分析和研究概括具有重要意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The choice of effect measure for binary outcomes: Introducing counterfactual outcome state transition parameters.

Standard measures of effect, including the risk ratio, the odds ratio, and the risk difference, are associated with a number of well-described shortcomings, and no consensus exists about the conditions under which investigators should choose one effect measure over another. In this paper, we introduce a new framework for reasoning about choice of effect measure by linking two separate versions of the risk ratio to a counterfactual causal model. In our approach, effects are defined in terms of "counterfactual outcome state transition parameters", that is, the proportion of those individuals who would not have been a case by the end of follow-up if untreated, who would have responded to treatment by becoming a case; and the proportion of those individuals who would have become a case by the end of follow-up if untreated who would have responded to treatment by not becoming a case. Although counterfactual outcome state transition parameters are generally not identified from the data without strong monotonicity assumptions, we show that when they stay constant between populations, there are important implications for model specification, meta-analysis, and research generalization.

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来源期刊
Epidemiologic Methods
Epidemiologic Methods Mathematics-Applied Mathematics
CiteScore
2.10
自引率
0.00%
发文量
7
期刊介绍: Epidemiologic Methods (EM) seeks contributions comparable to those of the leading epidemiologic journals, but also invites papers that may be more technical or of greater length than what has traditionally been allowed by journals in epidemiology. Applications and examples with real data to illustrate methodology are strongly encouraged but not required. Topics. genetic epidemiology, infectious disease, pharmaco-epidemiology, ecologic studies, environmental exposures, screening, surveillance, social networks, comparative effectiveness, statistical modeling, causal inference, measurement error, study design, meta-analysis
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